Chlorobutanol
|
|||
Names | |||
---|---|---|---|
IUPAC name
1,1,1-Trichloro-2-methylpropan-2-ol
|
|||
Other names
1,1,1-Trichloro-2-methyl-2-propanol; Chlorbutol; Chloreton; Chloretone; Chlortran; Trichloro-tert-butyl alcohol; 1,1,1-Trichloro-tert-butyl alcohol; 2-(Trichloromethyl)propan-2-ol, 1,1,1-trichloro-2-methyl-2-propanol; tert-Trichlorobutyl alcohol; Trichloro-tert-butanol; Trichlorisobutylalcohol; 2,2,2-Trichloro-1,1-dimethylethanol
|
|||
Identifiers | |||
57-15-8 ![]() |
|||
3D model (Jmol) | Interactive image | ||
ChEMBL | ChEMBL1439973 ![]() |
||
ChemSpider | 13842993 ![]() |
||
ECHA InfoCard | 100.000.288 | ||
KEGG | D01942 ![]() |
||
UNII | HM4YQM8WRC ![]() |
||
|
|||
|
|||
Properties | |||
C4H7Cl3O | |||
Molar mass | 177.45 g·mol−1 | ||
Appearance | White solid | ||
Odor | Menthol | ||
Melting point | 95–99 °C (203–210 °F; 368–372 K) | ||
Boiling point | 167 °C (333 °F; 440 K) | ||
Slightly soluble | |||
Solubility in acetone | Soluble | ||
Pharmacology | |||
A04AD04 (WHO) | |||
Hazards | |||
Main hazards | Xn | ||
NFPA 704 | |||
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
|
|||
![]() ![]() ![]() |
|||
Infobox references | |||
Chlorobutanol, or trichloro-2-methyl-2-propanol, is a chemical preservative, sedative hypnotic and weak local anaesthetic similar in nature to chloral hydrate. It has antibacterial and antifungal properties. Chlorobutanol is typically used at a concentration of 0.5% where it lends long term stability to multi-ingredient formulations. However, it retains antimicrobial activity at 0.05% in water. In pure state it is a white, volatile solid with a menthol-like odor.
Chemical synthesis[edit]
Chlorobutanol is formed by the simple nucleophilic addition of chloroform and acetone. The reaction is base driven by potassium or sodium hydroxide.
Toxicity[edit]
Chlorobutanol is highly toxic to the liver, is a skin irritant and a severe eye irritant.[1]
Parthenogenesis[edit]
Chlorobutanol has proven effective at stimulating parthenogenesis in sea urchin eggs up to the pluteus stage, possibly by increasing irritability to cause stimulation. For the eggs of the fish Oryzias latipes, however, chlorobutanol only acted as an anaesthetic.[2]